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Jump to: A | B | C | D | F | G | H | M | P | R | S | T | W | X
Number of items: 43.

A

An, SF and Ciardi, A and Giometto, B and Scaravilli, T and Gray, F and Scaravilli, F (1996) Investigation on the expression of major histocompatibility complex class II and cytokines and detection of HIV-1 DNA within brains of asymptomatic and symptomatic HIV-1-positive patients. ACTA NEUROPATHOL , 91 (5) 494 - 503.

An, SF and Giometto, B and Scaravilli, F (1996) HIV-1 DNA in brains in AIDS and pre-AIDS: Correlation with the stage of disease. ANN NEUROL , 40 (4) 611 - 617.

An, SF and Giometto, B and Scaravilli, T and Tavolato, B and Gray, F and Scaravilli, F (1996) Programmed cell death in brains of HIV-1-positive AIDS and pre-AIDS patients. ACTA NEUROPATHOL , 91 (2) 169 - 173.

B

Bandmann, O and Daniel, S and Marsden, CD and Wood, NW and Harding, AE (1996) The CTP-cyclohydrolase I gene in atypical Parkinsonian patients: A clinico-genetic study. J NEUROL SCI , 141 (1-2) 27 - 32.

Bandmann, O and Davis, MB and Marsden, CD and Wood, NW (1996) The human homologue of the weaver mouse gene in familial and sporadic Parkinson's disease. NEUROSCIENCE , 72 (4) 877 - 879.

Bandmann, O and Nygaard, TG and Surtees, R and Marsden, CD and Wood, NW and Harding, AE (1996) Dopa-responsive dystonia in British patients: New mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity. HUM MOL GENET , 5 (3) 403 - 406.

Barton, AJL and Crook, BW and Karran, EH and Brown, F and Dewar, D and Mann, DMA and Pearson, RCA and Graham, DI and Hardy, J and Hutton, M and Duff, K and Goate, AM and Clark, RF and Roberts, GW (1996) Alteration in brain presenilin 1 mRNA expression in early onset familial Alzheimer's disease. NEURODEGENERATION , 5 (3) 213 - 218. 10.1006/neur.1996.0029.

Bressman, SB and Warner, TT and Almasy, L and Uitti, RJ and Green, PE and Heiman, GA and Raymond, D and Ford, B and deLeon, D and Fahn, S and Kramer, PL and Risch, NJ and Maraganore, DM and Nygaard, TG and Harding, AE (1996) Exclusion of the DYT1 locus in familial torticollis. ANNALS OF NEUROLOGY , 40 (4) 681 - 684. 10.1002/ana.410400421.

C

Chalmers, RM and Davis, MB and Sweeney, MG and Wood, NW and Harding, AE (1996) Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy. AM J HUM GENET , 59 (1) 103 - 108.

Chu, FF and DeSilva, HAR and Esworthy, RS and Boteva, KK and Walters, CE and Roses, A and Rao, PN and Pettenati, MJ (1996) Polymorphism and chromosomal localization of the GI-form of human glutathione peroxidase (GPX2) on 14q24.1 by in situ hybridization. GENOMICS , 32 (2) 272 - 276. 10.1006/geno.1996.0115.

Clark, RF and Hutton, M and Talbot, C and Wragg, M and Lendon, C and Busfield, F and Han, SW and PerezTur, J and Adams, M and Fuldner, R and Roberts, G and Karran, E and Hardy, J and Goate, A (1996) The role of presenilin 1 in the genetics of Alzheimer's disease. In: COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY. (pp. 551 - 558).

Comi, GP and Ciafaloni, E and deSilva, HAR and Prelle, A and Bardoni, A and Rigoletto, C and Robotti, M and Bresolin, N and Moggio, M and Fortunato, F and Ciscato, P and Turconi, A and Roses, AD and Scarlato, G (1996) A G(+1)->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient (vol 4, pg 2171, 1995). HUMAN MOLECULAR GENETICS , 5 (4) 562 - 562.

D

David, G and Abbas, N and Coullin, P and Stevanin, G and Horta, W and Gemmill, R and Weissenbach, J and Wood, N and Cunha, S and Drabkin, H and Harding, AE and Agid, Y and Brice, A (1996) The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: Genetic and physical mapping of the SCA7 locus. AM J HUM GENET , 59 (6) 1328 - 1336.

David, G and Giunti, P and Abbas, N and Coullin, P and Stevanin, G and Horta, W and Gemmill, R and Weissenbach, J and Wood, N and Cunha, S and Drabkin, H and Harding, AE and Agid, Y and Brice, A (1996) The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus. Am J Hum Genet , 59 (6) 1328 - 1336.

David, K and Revesz, T and Path, MRC and Kratimenos, G and Krausz, T and Path, FRC and Crockard, HA (1996) Oncogenic osteomalacia associated with a meningeal phosphaturic mesenchymal tumor - Case report. J NEUROSURG , 84 (2) 288 - 292.

Davison, F and An, SF and Scaravilli, F (1996) Quantification of HIV DNA in the brain by PCR: Differences between fresh frozen and formalin fixed tissue. J CLIN PATHOL , 49 (5) 425 - 427.

Duff, K and Eckman, C and Zehr, C and Yu, X and Prada, CM and Pereztur, J and Hutton, M and Buee, L and Harigaya, Y and Yager, D and Morgan, D and Gordon, MN and Holcomb, L and Refolo, L and Zenk, B and Hardy, J and Younkin, S (1996) Increased amyloid-beta 42(43) in brains of mice expressing mutant presenilin 1. NATURE , 383 (6602) 710 - 713. 10.1038/383710a0.

F

Frontali, M and Sabbadini, G and Novelletto, A and Jodice, C and Naso, F and Spadaro, M and Giunti, P and Jacopini, AG and Veneziano, L and Mantuano, E and Malaspina, P and Ulizzi, L and Brice, A and Durr, A and Terrenato, L (1996) Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: A population genetics model for CAG repeat expansions. ANN HUM GENET , 60 423 - 435.

G

Geddes, JF and Thom, M and Robinson, SFD and Revesz, T (1996) Granular cell change in astrocytic tumors. AM J SURG PATHOL , 20 (1) 55 - 63.

Giometto, B and Scaravilli, T and Nicolao, P and An, SF and Groves, M and Tavolato, B and Beckett, AAJ and Scaravilli, F (1996) Detection of paraneoplastic anti-neuronal autoantibodies on paraffin-embedded tissues. ACTA NEUROPATHOL , 92 (5) 435 - 440.

H

Hardy, J (1996) New insights into the genetics of Alzheimer's disease. ANNALS OF MEDICINE , 28 (3) 255 - 258. 10.3109/07853899609033127.

Hutton, M and Busfield, F and Wragg, M and Crook, R and PerezTur, J and Clark, RF and Prihar, G and Talbot, C and Phillips, H and Wright, K and Baker, M and Lendon, C and Duff, K and Martinez, A and Houlden, H and Nichols, A and Karran, E and Roberts, G and Roques, P and Rossor, M and Venter, JC and Adams, MD and Cline, RT and Phillips, CA and Fuldner, RA and Hardy, J and Goate, A (1996) Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease. NEUROREPORT , 7 (3) 801 - 805.

M

Mann, DMA and Iwatsubo, T and Cairns, NJ and Lantos, PL and Nochlin, D and Sumi, SM and Bird, TD and Poorkaj, P and Hardy, J and Hutton, M and Prihar, G and Crook, R and Rossor, MN and Haltia, M (1996) Amyloid beta protein (A beta) deposition in chromosome 14-linked Alzheimer's disease: Predominance of A beta(42(43)). ANN NEUROL , 40 (2) 149 - 156.

Meckelein, B and deSilva, HAR and Roses, AD and Rao, PN and Pettenati, MJ and Xu, PT and Hodge, R and Glucksman, MJ and Abraham, CR (1996) Human endopeptidase (THOP1) is localized on chromosome 19 within the linkage region for the late-onset Alzheimer disease AD2 locus. GENOMICS , 31 (2) 246 - 249. 10.1006/geno.1996.0041.

P

Patel, AJ and Gunasekera, S and Jen, A and deSilva, HAR (1996) beta-amyloid-mediated inhibition of redox activity (MTT reduction) is not an indicator of astroglial degeneration. NEUROREPORT , 7 (12) 2026 - 2030. 10.1097/00001756-199608120-00035.

Patel, AJ and Wickenden, C and Jen, A and deSilva, HAR (1996) Glial cell derived neurotrophic factors and Alzheimer's disease. NEURODEGENERATION , 5 (4) 489 - 496. 10.1006/neur.1996.0068.

PerezTur, J and Croxton, R and Wright, K and Phillips, H and Zehr, C and Crook, R and Hutton, M and Hardy, J and Karran, E and Roberts, GW and Lancaster, S and Haltia, T (1996) A further presenilin 1 mutation in the exon 8 cluster in familial Alzheimer's disease. NEURODEGENERATION , 5 (3) 207 - 212. 10.1006/neur.1996.0028.

Prihar, G and Fuldner, RA and PerezTur, J and Lincoln, S and Duff, K and Crook, R and Hardy, J and Philips, CA and Venter, C and Talbot, C and Clark, RF and Goate, A and Li, JH and Potter, H and Karran, E and Roberts, GW and Hutton, M and Adams, MD (1996) Structure and alternative splicing of the presenilin-2 gene. NEUROREPORT , 7 (10) 1680 - 1684. 10.1097/00001756-199607080-00031.

R

Revesz, T and Sangha, H and Daniel, SE (1996) The nucleus raphe interpositus in progressive supranuclear palsy. J NEUROPATH EXP NEUR , 55 (5) 117 - 117.

Revesz, T and Sangha, H and Daniel, SE (1996) The nucleus raphe interpositus in the Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy). BRAIN , 119 1137 - 1143.

RiordanEva, P and Wood, NW (1996) Mitochondrial disorders in neuro-ophthalmology. CURR OPIN NEUROL , 9 (1) 1 - 4.

Royston, MC and Mann, D and PickeringBrown, S and Owen, F and Perry, R and Ragbavan, R and KhinNu, C and Tyner, S and Day, K and Crook, R and Hardy, J and Roberts, GW (1996) ApoE2 allele, Down's syndrome, and dementia. In: NEUROBIOLOGY OF ALZHEIMER'S DISEASE. (pp. 255 - 259).

Rudge, P and Webster, ADB and Revesz, T and Warner, T and Espanol, T and CunninghamRundles, C and Hyman, N (1996) Encephalomyelitis in primary hypogammaglobulinaemia. BRAIN , 119 1 - 15.

S

Saldanha, G and Holton, J and Pringle, H and Fletcher, A (1996) Cell death in dystrophic and inflammatory skeletal muscle disease: A central role for apoptosis? JOURNAL OF PATHOLOGY , 179 A27 - A27.

Scaravilli, F and An, SF and Ciardi, A and Giometto, B and Scaravilli, T and Gray, F (1996) Correlation between detection of HIV-1 DNA and expression of MHC II and cytokines in the brains of asymptomatic and symptomatic HIV-1 positive patients. J NEUROPATH EXP NEUR , 55 (5) 230 - 230.

Scheuner, D and Eckman, C and Jensen, M and Song, X and Citron, M and Suzuki, N and Bird, TD and Hardy, J and Hutton, M and Kukull, W and Larson, E and LevyLahad, E and Viitanen, M and Peskind, E and Poorkaj, P and Schellenberg, G and Tanzi, R and Wasco, W and Lannfelt, L and Selkoe, D and Younkin, S (1996) Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease. NATURE MEDICINE , 2 (8) 864 - 870. 10.1038/nm0896-864.

Seery, JP and Bryant, DJ and Schwieso, JE and Houlden, H and Changani, KK and Miles, G and Hodgson, HJF and TaylorRobinson, SD (1996) In vivo changes in hepatic phosphorus-31 and carbon-13 MR spectroscopy induced by intravenous intralipid infusion: Implications for the treatment of hepatic steatosis. GASTROENTEROLOGY , 110 (4) A1317 - A1317.

T

Talbot, C and Houlden, H and Craddock, N and Crook, R and Hutton, M and Lendon, C and Prihar, G and Morris, JC and Hardy, J and Goate, A (1996) Polymorphism in AACT gene may lower age of onset of Alzheimer's disease. NEUROREPORT , 7 (2) 534 - 536.

Thinakaran, G and Borchelt, DR and Lee, MK and Slunt, HH and Spitzer, L and Kim, G and Ratovitsky, T and Davenport, F and Nordstedt, C and Seeger, M and Hardy, J and Levey, AI and Gandy, SE and Jenkins, NA and Copeland, NG and Price, DL and Sisodia, SS (1996) Endoproteolysis of presenilin 1 and accumulation of processed derivatives in vivo. NEURON , 17 (1) 181 - 190. 10.1016/S0896-6273(00)80291-3.

Thom, M and Revesz, T (1996) Typical polyglucosan bodies are present in the sweat gland lumina in Lafora's disease. ACTA NEUROPATHOL , 92 (1) 102 - 103.

W

Ward, RV and Davis, JB and Gray, CW and Barton, AJL and Bresciani, LG and Caivano, M and Murphy, VF and Duff, K and Hutton, M and Hardy, J and Roberts, GW and Karran, EH (1996) Presenilin-1 is processed into two major cleavage products in neuronal cell lines. NEURODEGENERATION , 5 (4) 293 - 298. 10.1006/neur.1996.0040.

Wragg, M and Hutton, M and Talbot, C and Busfield, F and Han, SW and Lendon, C and Clark, RF and Morris, JC and Edwards, D and Goate, A and Pfeiffer, E and Crook, R and Prihar, G and Phillips, H and Baker, M and Hardy, J and Rossor, M and Houlden, H and Karran, E and Roberts, G and Craddock, N (1996) Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease. LANCET , 347 (9000) 509 - 512.

X

Xia, Y and deSilva, HAR and Rosi, BL and Yamaoka, LH and Rimmler, JB and PericakVance, MA and Roses, AD and Chen, X and Masliah, E and DeTeresa, R and Iwai, A and Sundsmo, M and Thomas, RG and Hofstetter, CR and Gregory, E and Hansen, LA and Katzman, R and Thal, LJ and Saitoh, T (1996) Genetic studies in Alzheimer's disease with an NACP/alpha-synuclein polymorphism. ANNALS OF NEUROLOGY , 40 (2) 207 - 215. 10.1002/ana.410400212.

This list was generated on Thu Jun 20 00:41:33 2013 BST.